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Not yet recruiting NCT07119632

Study of Medicine Stick Therapy Combined With Repeated Urotong Herapy on Lower Limb Dysfunction in Stroke Patients

No phase Interventional Stroke

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: RFE therapy.
Who it may be relevant to
Registry conditions: Stroke. Basic parameters: 18 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Clinical Study Plan of Medicine Stick Therapy Combined With Repeated Urotong Therapy on Lower Limb Dysfunction in Patients With Stroke

Overview

At present, domestic scholars have applied medicine stick therapy and repetitive facial exercise (RFE) to the rehabilitation treatment of stroke patients, but there are few relevant literature reports on medicine stick therapy combined with RFE and show the differences in the effects of the two different treatment methods. To this end, this study intends to follow up the effects and effects of drug stick therapy and its combined effect with RFE on the recovery of lower limb motor function in patients after stroke, and follow up the patients' limb motor function, daily life activity ability, quality of life, balance function, etc.

Detailed description

At present, domestic scholars have applied medicine stick therapy and repetitive facial exercise (RFE) to the rehabilitation treatment of stroke patients, but there are few relevant literature reports on medicine stick therapy combined with RFE and show the differences in the effects of the two different treatment methods. To this end, this study intends to follow up the effects and effects of drug stick therapy and its combined effect with RFE on the recovery of lower limb motor function in patients after stroke, and follow up the patients' limb motor function, daily life activity ability, quality of life, balance function, etc.; use the Fugl-Meyer motor function evaluation scale, Barthel index, Brunnstrom grading, Holden walking function and other scales to conduct multi-angle evaluation of stroke patients, combine traditional Chinese medicine rehabilitation with Western medicine rehabilitation treatment, combine these two different treatment technologies, give full play to their respective advantages and integrated effects to verify. The specific research content includes: participant recruitment and screening, random grouping design, baseline evaluation, treatment intervention, post-treatment evaluation, data statistics and analysis. This study aims to explore the feasibility and advantages of the combined application of drug stick therapy combined with RFE to provide more effective treatment methods for rehabilitation of stroke patients.

Interventions

  • Other RFE therapy

Primary outcome measures

  • Modified Barthel Index [Time frame: From enrollment to 8 weeks of treatment]
Secondary outcome measures (1)
  • Holden Walking Function [Time frame: From enrollment to 8 weeks of treatment]

Eligibility criteria

Inclusion criteria

  • Clinical diagnosis of stroke
  • The first onset and the disease duration must be less than 3 months. exclusion criteria:
  • Combined with other serious diseases such as severe cardiovascular, respiratory failure, liver and renal function damage, malignant tumors, etc.
  • Consciousness disorders and cognitive impairment;
  • Eczema, inflammation, infection, and scars at acupuncture points or skin;

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Quadruple blind
Primary purpose
Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07119632 · 2024B0564

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗